Colitose

Colitose
Skeletal formula of colitose
Ball-and-stick model of the colitose molecule
Names
IUPAC name
(2S,4S,5S)-2,4,5-trihydroxyhexanal
Identifiers
4221-05-0 YesY
ChemSpider 5256780 N
Jmol interactive 3D Image
PubChem 6857442
Properties
C6H12O4
Molar mass 148.15 g/mol
Density 1.25 g/mL
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Colitose (or GDP-colitose) is a mannose-derived 3,6-dideoxysugar produced by certain bacteria. It is a constituent of the lipopolysaccharide.[1]

Biological role

Colitose is found in the O-antigen of certain Gram-negative bacteria such as Escherichia coli, Yersinia pseudotuberculosis, Salmonella enterica, Vibrio cholerae, and in marine bacteria such as Pseudoalteromonas sp.[2][1] The sugar was first isolated in 1958,[3] and subsequently was enzymatically synthesized in 1962.[4]

Biosynthesis

The GDP-L-colitose biosynthesis pathway. For clarity, groups modified by the previous enzymatic step are highlighted in yellow.

The biosynthesis of colitose begins with ColE, a mannose-1-phosphate guanylyltransferase that catalyzes the addition of a GMP moiety to mannose, yielding GDP-mannose. In the next step, ColB, an NADP-dependent short-chain dehydrogenase-reductase enzyme, catalyzes the oxidation at C-4 and the removal of the hydroxyl group at C-6. The resulting product, GDP-4-keto-6-deoxymannose, then reacts with the PLP-dependent enzyme GDP-4-keto-6-deoxymannose-3-dehydratase (ColD), which removes the hydroxyl at C-3 in a manner similar to that of serine dehydratase. In the final step, the product of ColD, GDP-4-keto-3,6-dideoxymannose, reacts with ColC, which reduces the ketone functionality at C-4 back to an alcohol and inverts the configuration about C-5.[5]

The resulting product, GDP-L-colitose, is then incorporated into the O-antigen by glycosyltransferases and O-antigen processing proteins. Further reactions join the O-antigen to the core polysaccharide to form the full lipopolysaccharide.

GDP-4-keto-6-deoxymannose-3-dehydratase (ColD)

ColD is a PLP-dependent enzyme responsible for the removal of the C-3' hydroxyl group during the biosynthesis of GDP-colitose.[5] It is a product of the Wbdk or ColD genes in Escherichia coli O55 or Salmonella enterica, respectively, and is commonly referred to as ColD.[1]

Usage in biotechnology

Although the sugar is relatively rare, recent work with glycosyltransferases suggests that obscure sugars such as colitose can be incorporated into existing natural-product scaffolds, thereby constructing novel and potentially therapeutic compounds.[6]

References

  1. 1 2 3 Samuel G, Reeves P (November 2003). "Biosynthesis of O-antigens: genes and pathways involved in nucleotide sugar precursor synthesis and O-antigen assembly". Carbohydrate Research 338 (23): 2503–19. doi:10.1016/j.carres.2003.07.009. PMID 14670712.
  2. ↑ Muldoon J, Perepelov AV, Shashkov AS; et al. (June 2001). "Structure of a colitose-containing O-specific polysaccharide of the marine bacterium Pseudoalteromonas tetraodonis IAM 14160(T)". Carbohydrate Research 333 (1): 41–6. doi:10.1016/S0008-6215(01)00121-5. PMID 11423109.
  3. ↑ Luderitz O, Staub AM, Stirm S, Westphal O (1958). "[Colitose, 3-desoxy-L-fucose, a new sugar building block with immunospecific functions in the endotoxins, lipopolysaccharides, of some gram-negative bacteria.]". Biochemische Zeitschrift (in German) 330 (3): 193–7. PMID 13546193.
  4. ↑ Heath EC, ELBEIN AD (July 1962). "The enzymatic synthesis of guanosine diphosphate colitose by a mutant strain of Escherichia coli". Proceedings of the National Academy of Sciences of the United States of America 48: 1209–16. doi:10.1073/pnas.48.7.1209. PMC 220934. PMID 13905784.
  5. 1 2 Alam J, Beyer N, Liu HW (December 2004). "Biosynthesis of colitose: expression, purification, and mechanistic characterization of GDP-4-keto-6-deoxy-D-mannose-3-dehydrase (ColD) and GDP-L-colitose synthase (ColC)". Biochemistry 43 (51): 16450–60. doi:10.1021/bi0483763. PMID 15610039.
  6. ↑ Zhang C, Griffith BR, Fu Q; et al. (September 2006). "Exploiting the reversibility of natural product glycosyltransferase-catalyzed reactions". Science 313 (5791): 1291–4. doi:10.1126/science.1130028. PMID 16946071.
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